BMS-214662 mesylate

CAS: 474010-58-7 F: C26H27N5O5S3 W: 585.72

BMS-214662 mesylate is a potent and selective farnesyl transferase inhibitor with an IC50 of 1.35 nM. BMS-214662 mesylat

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Bioactivity	BMS-214662 mesylate is a potent and selective farnesyl transferase inhibitor with an IC50 of 1.35 nM. BMS-214662 mesylate exhibits potent antitumor activity and can be utilized in cancer research[1].
Invitro	BMS-214662 对法尼基转移酶的选择性超过 1000 倍，抑制 Ras-CVLL 和 K-Ras 的香叶基香叶基化的 IC50 值分别为 1.3 和 2.3 μM[1]。BMS-214662 在抑制 H-ras 转化的啮齿动物细胞、A2780 人卵巢癌肿瘤细胞和 HCT-116 人结肠癌肿瘤细胞方面表现出良好的效力。BMS-214662 是已知最有效的凋亡 FTI，对一组具有不同组织学的细胞系表现出广谱但强大的细胞选择性细胞毒活性[2]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> BMS-214662 mesylate 相关抗体:
In Vivo	与未处理的对照小鼠相比，经 BMS-214662 处理的小鼠肿瘤中的凋亡细胞数量增加。与未处理的对照组相比，BMS-214662 处理的小鼠中 HCT-116 肿瘤的 AI 增加了 4-10 倍。BMS-214662 对 HCT-116 和 EJ-1 肿瘤细胞均具有显著的细胞毒性；对于 HCT-116 和 EJ-1 肿瘤，杀死 90% 克隆形成肿瘤细胞所需的 BMS-214662 剂量约为 75 和 100 mg/kg[2]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only.
CAS	474010-58-7
Formula	C26H27N5O5S3
Molar Mass	585.72
Transport	Room temperature in continental US; may vary elsewhere.
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.
Reference	[1]. Hunt JT, et al. Discovery of (R)-7-cyano-2,3,4, 5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-3- (phenylmethyl)-4-(2-thienylsulfonyl)-1H-1,4-benzodiazepine (BMS-214662), a farnesyltransferase inhibitor with potent preclinical antitumor activity. J Med Chem. 2000 Oct 5;43(20):3587-95. [2]. Rose WC, et al. Preclinical antitumor activity of BMS-214662, a highly apoptotic and novel farnesyltransferase inhibitor. Cancer Res. 2001 Oct 15;61(20):7507-17.

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